A clinical trial to evaluate the effect of an Ayurvedic medicine, varyadi kashaya in patients with raised blood levels of uric acid.
Phase 2
- Conditions
- Health Condition 1: M109- Gout, unspecified
- Registration Number
- CTRI/2023/03/050452
- Lead Sponsor
- INSTITUTE OF POST GRADUATE AYURVEDIC EDUCATION AND RESEARCH AT S.V.S.P.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
PATIENTS HAVING CLASSICAL SYMPTOMS OF VATARAKTA(GOUT) WILL BE SELECTED FROM OPD AND IPD.
TODA (PRICKING PAIN)
BHEDA (TEARING PAIN)
DAHA (BURNING SENSATION)
SUPTI (NUMBNESS)
SOPHA (SWELLING)
RAGA (REDNESS)
Exclusion Criteria
PATIENTS BELLOW 20 AND ABOVE 65 YEARS OF AGE.
PATIENTS WITH HEART DISEASE, MALIGNANCY, PREGNANT, SEVERE RENAL DISEASE, SEVERE HEPATIC DISEASE AND ANY OTHER CONDITION WHICH THE PRINCIPAL INVESTIGATOR THINKS MAY JEOPARDIZE THE STUDY.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method MEAN PERCENTAGE DECREASE IN SERUM URIC ACID LEVEL FROM THE BASELINE TO THE END OF STUDY.Timepoint: DECREASE THE SERUM URIC ACID LEVEL AFTER 15 DAYS AND 30 DAYS OF TREATMENT.
- Secondary Outcome Measures
Name Time Method RELIEF IN THE CLINICAL SYMPTOMS OF VATARAKTA (GOUT) <br/ ><br>TODA (PRICKING PAIN) <br/ ><br>BHEDA (TEARING PAIN) <br/ ><br>DAHA (BURNING SENSATION) <br/ ><br>SUPTI (NUMBNESS) <br/ ><br>SOPHA (SWELLING) <br/ ><br>RAGA (REDNESS)Timepoint: UPTO 30 DAYS